<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">nogr</journal-id><journal-title-group><journal-title xml:lang="ru">Экспериментальная и клиническая гастроэнтерология</journal-title><trans-title-group xml:lang="en"><trans-title>Experimental and Clinical Gastroenterology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1682-8658</issn><publisher><publisher-name>«Global Media Technologies»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.31146/1682-8658-ecg-205-9-129-139</article-id><article-id custom-type="elpub" pub-id-type="custom">nogr-2049</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОБЗОР</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEW</subject></subj-group></article-categories><title-group><article-title>Основы иммуноонкологии и иммунотерапии в онкологии</article-title><trans-title-group xml:lang="en"><trans-title>Basics of immunooncology and immunotherapy in oncology</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Логинова</surname><given-names>Екатерина Николаевна</given-names></name><name name-style="western" xml:lang="en"><surname>Loginova</surname><given-names>E. N.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лялюкова</surname><given-names>Елена Александровна</given-names></name><name name-style="western" xml:lang="en"><surname>Lyalyukova</surname><given-names>E. A.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0440-7118</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Надей</surname><given-names>Елена Витальевна</given-names></name><name name-style="western" xml:lang="en"><surname>Nadey</surname><given-names>E. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Семенова</surname><given-names>Елена Владимировна</given-names></name><name name-style="western" xml:lang="en"><surname>Semenova</surname><given-names>E. V.</given-names></name></name-alternatives><email xlink:type="simple">sel.92@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБОУ ВО «Омский государственный медицинский университет» Министерства здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Omsk State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>07</day><month>10</month><year>2022</year></pub-date><volume>0</volume><issue>9</issue><fpage>129</fpage><lpage>139</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Логинова Е.Н., Лялюкова Е.А., Надей Е.В., Семенова Е.В., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Логинова Е.Н., Лялюкова Е.А., Надей Е.В., Семенова Е.В.</copyright-holder><copyright-holder xml:lang="en">Loginova E.N., Lyalyukova E.A., Nadey E.V., Semenova E.V.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.nogr.org/jour/article/view/2049">https://www.nogr.org/jour/article/view/2049</self-uri><abstract><p>Цель обзора - представить анализ современных литературных данных о иммунологии опухоли, эффекторных механизмах противоопухолевого иммунитета, перспективах разработки новых иммунотерапевтических подходов к лечению рака. Иммунололгический надзор - интеллектуальная основа идеи иммунологии опухолей. Ни у кого не вызывает сомнений роль иммунологических механизмов в защите от опухолей. Однако, опухолевые клетки располагают разнообразными механизмами, позволяющими им избежать действия факторов иммунного надзора. Некоторые из этих факторов направлены на затруднение распознавания чужеродных компонентов в составе опухоли и запуска иммунных процессов. Другие механизмы препятствуют реализации эффекторных механизмов. Понимание механизмов иммунологического ускользания может предложить механизмы иммунной терапии, которые будут широко применимы для разных типов рака.</p></abstract><trans-abstract xml:lang="en"><p>The purpose of the review is to present an analysis of current literature data on tumor immunology, effector mechanisms of antitumor immunity, and prospects for the development of new immunotherapeutic approaches to cancer treatment. Immunological surveillance is the intellectual basis of the idea of tumor immunology. No one doubts the role of immunological mechanisms in protection against tumors. However, tumor cells have a variety of mechanisms that allow them to avoid the action of immune surveillance factors. Some of these factors are aimed at making it difficult to recognize foreign components in the tumor and trigger immune processes. Other mechanisms prevent the implementation of effector mechanisms. Understanding the mechanisms of immunological escape may suggest immune therapy mechanisms that will be widely applicable to different types of cancer.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>иммунный ответ</kwd><kwd>опухоль</kwd><kwd>иммунитет</kwd><kwd>рак</kwd><kwd>лимфоцит</kwd><kwd>киллер</kwd><kwd>терапия</kwd><kwd>цитокины</kwd><kwd>вирусы</kwd><kwd>клетки</kwd></kwd-group><kwd-group xml:lang="en"><kwd>immune response</kwd><kwd>tumor</kwd><kwd>immunity</kwd><kwd>cancer</kwd><kwd>lymphocyte</kwd><kwd>killer</kwd><kwd>therapy</kwd><kwd>cytokines</kwd><kwd>viruses</kwd><kwd>cells</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Coley W. B. The treatment of malignant tumors by repeated inoculations of erysipelas: with a report of ten original cases. Am J Med Sci. 1893; 105:487. PMID: 1984929</mixed-citation><mixed-citation xml:lang="en">Coley W. B. The treatment of malignant tumors by repeated inoculations of erysipelas: with a report of ten original cases. Am J Med Sci. 1893; 105:487. PMID: 1984929</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Gras Navarro A., Björklund A. T., Chekenya M. Therapeutic potential and challenges of natural killer cells in treatment of solid tumors. Front Immunol. 2015; 6:202. doi: 10.3389/fimmu.2015.00202.</mixed-citation><mixed-citation xml:lang="en">Gras Navarro A., Björklund A. T., Chekenya M. Therapeutic potential and challenges of natural killer cells in treatment of solid tumors. Front Immunol. 2015; 6:202. doi: 10.3389/fimmu.2015.00202.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Savage P.A., Leventhal D. S., Malchow S. Shaping the repertoire of tumor-infiltrating effector and regulatory T cells. Immunol Rev. 2014; 259:245. doi: 10.1111/imr.12166.</mixed-citation><mixed-citation xml:lang="en">Savage P.A., Leventhal D. S., Malchow S. Shaping the repertoire of tumor-infiltrating effector and regulatory T cells. Immunol Rev. 2014; 259:245. doi: 10.1111/imr.12166.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Marvel D., Gabrilovich D. I. Myeloid-derived suppressor cells in the tumor microenvironment: expect the unexpected. J Clin Invest. 2015; 125:3356. doi: 10.1172/JCI80005.</mixed-citation><mixed-citation xml:lang="en">Marvel D., Gabrilovich D. I. Myeloid-derived suppressor cells in the tumor microenvironment: expect the unexpected. J Clin Invest. 2015; 125:3356. doi: 10.1172/JCI80005.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Bailey S.R., Nelson M. H., Himes R. A., et al. Th17 cells in cancer: the ultimate identity crisis. Front Immunol. 2014; 5:276. doi: 10.3389/fimmu.2014.00276.</mixed-citation><mixed-citation xml:lang="en">Bailey S.R., Nelson M. H., Himes R. A., et al. Th17 cells in cancer: the ultimate identity crisis. Front Immunol. 2014; 5:276. doi: 10.3389/fimmu.2014.00276.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Laoui D., Van Overmeire E., De Baetselier P., et al. Functional Relationship between Tumor-Associated Macrophages and Macrophage Colony-Stimulating Factor as Contributors to Cancer Progression. Front Immunol. 2014; 5:489. doi: 10.3389/fimmu.2014.00489.</mixed-citation><mixed-citation xml:lang="en">Laoui D., Van Overmeire E., De Baetselier P., et al. Functional Relationship between Tumor-Associated Macrophages and Macrophage Colony-Stimulating Factor as Contributors to Cancer Progression. Front Immunol. 2014; 5:489. doi: 10.3389/fimmu.2014.00489.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">van der Merwe P. A., Dushek O. Mechanisms for T cell receptor triggering. Nat Rev Immunol. 2011; 11:47. doi: 10.1038/nri2887.</mixed-citation><mixed-citation xml:lang="en">van der Merwe P. A., Dushek O. Mechanisms for T cell receptor triggering. Nat Rev Immunol. 2011; 11:47. doi: 10.1038/nri2887.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Hennecke J., Wiley D. C. T cell receptor-MHC interactions up close. Cell. 2001; 104:1. oi: 10.1016/s0092-8674(01)00185-4.</mixed-citation><mixed-citation xml:lang="en">Hennecke J., Wiley D. C. T cell receptor-MHC interactions up close. Cell. 2001; 104:1. oi: 10.1016/s0092-8674(01)00185-4.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Schwartz R.H. A cell culture model for T lymphocyte clonal anergy. Science. 1990; 248:1349. doi: 10.1126/science.2113314.</mixed-citation><mixed-citation xml:lang="en">Schwartz R.H. A cell culture model for T lymphocyte clonal anergy. Science. 1990; 248:1349. doi: 10.1126/science.2113314.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Wherry E.J. T cell exhaustion. Nat Immunol. 2011; 12:492. doi: 10.1038/ni.2035.</mixed-citation><mixed-citation xml:lang="en">Wherry E.J. T cell exhaustion. Nat Immunol. 2011; 12:492. doi: 10.1038/ni.2035.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Schreiber R.D, Old LJ, Smyth MJ. Cancer immunoediting: integrating immunity’s roles in cancer suppression and promotion. Science. 2011; 331:1565. DOI: 10.1126/science.1203486</mixed-citation><mixed-citation xml:lang="en">Schreiber R.D, Old LJ, Smyth MJ. Cancer immunoediting: integrating immunity’s roles in cancer suppression and promotion. Science. 2011; 331:1565. DOI: 10.1126/science.1203486</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Tran E., Turcotte S., Gros A., et al. Cancer immunotherapy based on mutation-specific CD4+ T cells in a patient with epithelial cancer. Science. 2014; 344:641. doi: 10.1126/science.1251102.</mixed-citation><mixed-citation xml:lang="en">Tran E., Turcotte S., Gros A., et al. Cancer immunotherapy based on mutation-specific CD4+ T cells in a patient with epithelial cancer. Science. 2014; 344:641. doi: 10.1126/science.1251102.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Matsushita H., Vesely M. D., Koboldt D. C., et al. Cancer exome analysis reveals a T-cell-dependent mechanism of cancer immunoediting. Nature. 2012; 482:400. doi: 10.1038/nature10755.</mixed-citation><mixed-citation xml:lang="en">Matsushita H., Vesely M. D., Koboldt D. C., et al. Cancer exome analysis reveals a T-cell-dependent mechanism of cancer immunoediting. Nature. 2012; 482:400. doi: 10.1038/nature10755.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Vinay D.S., Ryan E. P., Pawelec G., et al. Immune evasion in cancer: Mechanistic basis and therapeutic strategies. Semin Cancer Biol. 2015; 35 Suppl: S185. doi: 10.1016/j.semcancer.2015.03.004.</mixed-citation><mixed-citation xml:lang="en">Vinay D.S., Ryan E. P., Pawelec G., et al. Immune evasion in cancer: Mechanistic basis and therapeutic strategies. Semin Cancer Biol. 2015; 35 Suppl: S185. doi: 10.1016/j.semcancer.2015.03.004.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Johnsen A.K., Templeton D. J., Sy M., Harding C. V. Deficiency of transporter for antigen presentation (TAP) in tumor cells allows evasion of immune surveillance and increases tumorigenesis. J Immunol. 1999; 163:4224. PMID: 10510359</mixed-citation><mixed-citation xml:lang="en">Johnsen A.K., Templeton D. J., Sy M., Harding C. V. Deficiency of transporter for antigen presentation (TAP) in tumor cells allows evasion of immune surveillance and increases tumorigenesis. J Immunol. 1999; 163:4224. PMID: 10510359</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Donia M., Andersen R., Kjeldsen J. W., et al. Aberrant Expression of MHC Class II in Melanoma Attracts Inflammatory Tumor-Specific CD4+ T- Cells, Which Dampen CD8+ T-cell Antitumor Reactivity. Cancer Res. 2015; 75:3747. doi: 10.1158/0008-5472.CAN-14-2956.</mixed-citation><mixed-citation xml:lang="en">Donia M., Andersen R., Kjeldsen J. W., et al. Aberrant Expression of MHC Class II in Melanoma Attracts Inflammatory Tumor-Specific CD4+ T- Cells, Which Dampen CD8+ T-cell Antitumor Reactivity. Cancer Res. 2015; 75:3747. doi: 10.1158/0008-5472.CAN-14-2956.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Rooney M.S., Shukla S. A., Wu C. J., et al. Molecular and genetic properties of tumors associated with local immune cytolytic activity. Cell 2015; 160:48. Rooney MS, Shukla SA, Wu CJ, et al. Molecular and genetic properties of tumors associated with local immune cytolytic activity. Cell. 2015; 160:48. doi: 10.1016/j.cell.2014.12.033.</mixed-citation><mixed-citation xml:lang="en">Rooney M.S., Shukla S. A., Wu C. J., et al. Molecular and genetic properties of tumors associated with local immune cytolytic activity. Cell 2015; 160:48. Rooney MS, Shukla SA, Wu CJ, et al. Molecular and genetic properties of tumors associated with local immune cytolytic activity. Cell. 2015; 160:48. doi: 10.1016/j.cell.2014.12.033.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Catalán E., Charni S., Jaime P., et al. MHC-I modulation due to changes in tumor cell metabolism regulates tumor sensitivity to CTL and NK cells. Oncoimmunology. 2015; 4: e985924. doi: 10.4161/2162402X.2014.985924.</mixed-citation><mixed-citation xml:lang="en">Catalán E., Charni S., Jaime P., et al. MHC-I modulation due to changes in tumor cell metabolism regulates tumor sensitivity to CTL and NK cells. Oncoimmunology. 2015; 4: e985924. doi: 10.4161/2162402X.2014.985924.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Reichel J., Chadburn A., Rubinstein P. G., et al. Flow sorting and exome sequencing reveal the oncogenome of primary Hodgkin and Reed-Sternberg cells. Blood. 2015; 125:1061. doi: 10.1182/blood-2014-11-610436</mixed-citation><mixed-citation xml:lang="en">Reichel J., Chadburn A., Rubinstein P. G., et al. Flow sorting and exome sequencing reveal the oncogenome of primary Hodgkin and Reed-Sternberg cells. Blood. 2015; 125:1061. doi: 10.1182/blood-2014-11-610436</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Zaretsky J.M., Garcia-Diaz A., Shin D. S., et al. Mutations Associated with Acquired Resistance to PD-1 Blockade in Melanoma. N Engl J Med. 2016; 375:819. DOI: 10.1056/NEJMoa1604958</mixed-citation><mixed-citation xml:lang="en">Zaretsky J.M., Garcia-Diaz A., Shin D. S., et al. Mutations Associated with Acquired Resistance to PD-1 Blockade in Melanoma. N Engl J Med. 2016; 375:819. DOI: 10.1056/NEJMoa1604958</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Amend S.R., Pienta K. J. Ecology meets cancer biology: the cancer swamp promotes the lethal cancer phenotype. Oncotarget. 2015; 6:9669. DOI: 10.18632/oncotarget.3430.</mixed-citation><mixed-citation xml:lang="en">Amend S.R., Pienta K. J. Ecology meets cancer biology: the cancer swamp promotes the lethal cancer phenotype. Oncotarget. 2015; 6:9669. DOI: 10.18632/oncotarget.3430.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Guo F., Wang Y., Liu J., et al. CXCL12/CXCR4: a symbiotic bridge linking cancer cells and their stromal neighbors in oncogenic communication networks. Oncogene. 2016; 35:816. doi: 10.1038/onc.2015.139.</mixed-citation><mixed-citation xml:lang="en">Guo F., Wang Y., Liu J., et al. CXCL12/CXCR4: a symbiotic bridge linking cancer cells and their stromal neighbors in oncogenic communication networks. Oncogene. 2016; 35:816. doi: 10.1038/onc.2015.139.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Tumeh P.C., Harview C. L., Yearley J. H., et al. PD-1 blockade induces responses by inhibiting adaptive immune resistance. Nature. 2014; 515:568. doi: 10.1038/nature13954.</mixed-citation><mixed-citation xml:lang="en">Tumeh P.C., Harview C. L., Yearley J. H., et al. PD-1 blockade induces responses by inhibiting adaptive immune resistance. Nature. 2014; 515:568. doi: 10.1038/nature13954.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Balachandran V.P., Cavnar M. J., Zeng S., et al. Imatinib potentiates antitumor T cell responses in gastrointestinal stromal tumor through the inhibition of Ido. Nat Med. 2011; 17:1094. doi: 10.1038/nm.2438.</mixed-citation><mixed-citation xml:lang="en">Balachandran V.P., Cavnar M. J., Zeng S., et al. Imatinib potentiates antitumor T cell responses in gastrointestinal stromal tumor through the inhibition of Ido. Nat Med. 2011; 17:1094. doi: 10.1038/nm.2438.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Spranger S., Bao R., Gajewski T. F. Melanoma-intrinsic β-catenin signalling prevents anti-tumour immunity. Nature. 2015; 523:231. doi: 10.1038/nature14404.</mixed-citation><mixed-citation xml:lang="en">Spranger S., Bao R., Gajewski T. F. Melanoma-intrinsic β-catenin signalling prevents anti-tumour immunity. Nature. 2015; 523:231. doi: 10.1038/nature14404.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Boyman O., Sprent J. The role of interleukin-2 during homeostasis and activation of the immune system. Nat Rev Immunol. 2012; 12:180. doi: 10.1038/nri3156.</mixed-citation><mixed-citation xml:lang="en">Boyman O., Sprent J. The role of interleukin-2 during homeostasis and activation of the immune system. Nat Rev Immunol. 2012; 12:180. doi: 10.1038/nri3156.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Krieg C., Létourneau S., Pantaleo G., Boyman O. Improved IL-2 immunotherapy by selective stimulation of IL-2 receptors on lymphocytes and endothelial cells. Proc Natl Acad Sci USA. 2010; 107:11906. doi:10.1073/pnas.1002569107</mixed-citation><mixed-citation xml:lang="en">Krieg C., Létourneau S., Pantaleo G., Boyman O. Improved IL-2 immunotherapy by selective stimulation of IL-2 receptors on lymphocytes and endothelial cells. Proc Natl Acad Sci USA. 2010; 107:11906. doi:10.1073/pnas.1002569107</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Zeiser R., Nguyen V. H., Beilhack A., et al. Inhibition of CD4+CD25+ regulatory T-cell function by calcineurin-dependent interleukin-2 production. Blood. 2006; 108:390. doi: 10.1182/blood-2006-01-0329.</mixed-citation><mixed-citation xml:lang="en">Zeiser R., Nguyen V. H., Beilhack A., et al. Inhibition of CD4+CD25+ regulatory T-cell function by calcineurin-dependent interleukin-2 production. Blood. 2006; 108:390. doi: 10.1182/blood-2006-01-0329.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Laurence A., Tato C. M., Davidson T. S., et al.Interleukin-2 signaling via STAT5 constrains T helper 17 cell generation. Immunity. 2007; 26:371. doi: 10.1016/j.immuni.2007.02.009.</mixed-citation><mixed-citation xml:lang="en">Laurence A., Tato C. M., Davidson T. S., et al.Interleukin-2 signaling via STAT5 constrains T helper 17 cell generation. Immunity. 2007; 26:371. doi: 10.1016/j.immuni.2007.02.009.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Kryczek I., Wei S., Zou L., et al. Cutting edge: Th17 and regulatory T cell dynamics and the regulation by IL-2 in the tumor microenvironment. J Immunol. 2007; 178:6730. doi: 10.4049/jimmunol.178.11.6730.</mixed-citation><mixed-citation xml:lang="en">Kryczek I., Wei S., Zou L., et al. Cutting edge: Th17 and regulatory T cell dynamics and the regulation by IL-2 in the tumor microenvironment. J Immunol. 2007; 178:6730. doi: 10.4049/jimmunol.178.11.6730.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Rosenberg S.A., Yang J. C., Topalian S. L., et al. Treatment of 283 consecutive patients with metastatic melanoma or renal cell cancer using high-dose bolus interleukin 2. JAMA. 1994; 271:907. PMID: 8120958.</mixed-citation><mixed-citation xml:lang="en">Rosenberg S.A., Yang J. C., Topalian S. L., et al. Treatment of 283 consecutive patients with metastatic melanoma or renal cell cancer using high-dose bolus interleukin 2. JAMA. 1994; 271:907. PMID: 8120958.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Atkins M.B., Lotze M. T., Dutcher J. P., et al. High-dose recombinant interleukin 2 therapy for patients with metastatic melanoma: analysis of 270 patients treated between 1985 and 1993. J Clin Oncol. 1999; 17:2105. doi: 10.1200/JCO.1999.17.7.2105.</mixed-citation><mixed-citation xml:lang="en">Atkins M.B., Lotze M. T., Dutcher J. P., et al. High-dose recombinant interleukin 2 therapy for patients with metastatic melanoma: analysis of 270 patients treated between 1985 and 1993. J Clin Oncol. 1999; 17:2105. doi: 10.1200/JCO.1999.17.7.2105.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Lu G., Middleton R. E., Sun H., et al. The myeloma drug lenalidomide promotes the cereblon-dependent destruction of Ikaros proteins. Science. 2014; 343:305. doi: 10.1126/science.1244917.</mixed-citation><mixed-citation xml:lang="en">Lu G., Middleton R. E., Sun H., et al. The myeloma drug lenalidomide promotes the cereblon-dependent destruction of Ikaros proteins. Science. 2014; 343:305. doi: 10.1126/science.1244917.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Avitahl N., Winandy S., Friedrich C., et al. Ikaros sets thresholds for T cell activation and regulates chromosome propagation. Immunity. 1999; 10:333. doi: 10.1016/s1074-7613(00)80033-3.</mixed-citation><mixed-citation xml:lang="en">Avitahl N., Winandy S., Friedrich C., et al. Ikaros sets thresholds for T cell activation and regulates chromosome propagation. Immunity. 1999; 10:333. doi: 10.1016/s1074-7613(00)80033-3.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Quintana F.J., Jin H., Burns E. J., et al. Aiolos promotes TH17 differentiation by directly silencing Il2 expression. Nat Immunol. 2012; 13:770. doi: 10.1038/ni.2363.</mixed-citation><mixed-citation xml:lang="en">Quintana F.J., Jin H., Burns E. J., et al. Aiolos promotes TH17 differentiation by directly silencing Il2 expression. Nat Immunol. 2012; 13:770. doi: 10.1038/ni.2363.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Lesinski G.B., Anghelina M., Zimmerer J., et al. The antitumor effects of IFN-alpha are abrogated in a STAT1-deficient mouse. J Clin Invest. 2003; 112:170. doi: 10.1172/JCI16603.</mixed-citation><mixed-citation xml:lang="en">Lesinski G.B., Anghelina M., Zimmerer J., et al. The antitumor effects of IFN-alpha are abrogated in a STAT1-deficient mouse. J Clin Invest. 2003; 112:170. doi: 10.1172/JCI16603.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Carson W. E.Interferon-alpha-induced activation of signal transducer and activator of transcription proteins in malignant melanoma. Clin Cancer Res. 1998; 4:2219. PMID: 9748142</mixed-citation><mixed-citation xml:lang="en">Carson W. E.Interferon-alpha-induced activation of signal transducer and activator of transcription proteins in malignant melanoma. Clin Cancer Res. 1998; 4:2219. PMID: 9748142</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Weber J., Mandala M., Del Vecchio M., et al. Adjuvant Nivolumab versus Ipilimumab in Resected Stage III or IV Melanoma. N Engl J Med. 2017; 377:1824. doi: 10.1056/NEJMoa1709030.</mixed-citation><mixed-citation xml:lang="en">Weber J., Mandala M., Del Vecchio M., et al. Adjuvant Nivolumab versus Ipilimumab in Resected Stage III or IV Melanoma. N Engl J Med. 2017; 377:1824. doi: 10.1056/NEJMoa1709030.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Eggermont A.M., Chiarion-Sileni V., Grob J. J., et al. Prolonged Survival in Stage III Melanoma with Ipilimumab Adjuvant Therapy. N Engl J Med. 2016; 375:1845. doi: 10.1056/NEJMoa1611299.</mixed-citation><mixed-citation xml:lang="en">Eggermont A.M., Chiarion-Sileni V., Grob J. J., et al. Prolonged Survival in Stage III Melanoma with Ipilimumab Adjuvant Therapy. N Engl J Med. 2016; 375:1845. doi: 10.1056/NEJMoa1611299.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Redelman-Sidi G., Glickman M. S., Bochner B. H. The mechanism of action of BCG therapy for bladder cancer - a current perspective. Nat Rev Urol. 2014; 11:153. doi: 10.1038/nrurol.2014.15.</mixed-citation><mixed-citation xml:lang="en">Redelman-Sidi G., Glickman M. S., Bochner B. H. The mechanism of action of BCG therapy for bladder cancer - a current perspective. Nat Rev Urol. 2014; 11:153. doi: 10.1038/nrurol.2014.15.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Francisco L.M., Salinas V. H., Brown K. E., et al. PD-L1 regulates the development, maintenance, and function of induced regulatory T cells. J Exp Med. 2009; 206:3015. doi: 10.1084/jem.20090847.</mixed-citation><mixed-citation xml:lang="en">Francisco L.M., Salinas V. H., Brown K. E., et al. PD-L1 regulates the development, maintenance, and function of induced regulatory T cells. J Exp Med. 2009; 206:3015. doi: 10.1084/jem.20090847.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Amarnath S., Mangus C. W., Wang J. C., et al. The PDL1-PD1 axis converts human TH1 cells into regulatory T cells. Sci Transl Med. 2011; 3:111ra120. doi: 10.1126/scitranslmed.3003130</mixed-citation><mixed-citation xml:lang="en">Amarnath S., Mangus C. W., Wang J. C., et al. The PDL1-PD1 axis converts human TH1 cells into regulatory T cells. Sci Transl Med. 2011; 3:111ra120. doi: 10.1126/scitranslmed.3003130</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Spranger S., Spaapen R. M., Zha Y., et al. Up-regulation of PD-L1, IDO, and T(regs) in the melanoma tumor microenvironment is driven by CD8(+) T cells. Sci Transl Med. 2013; 5:200ra116. doi: 10.1126/scitranslmed.3006504.</mixed-citation><mixed-citation xml:lang="en">Spranger S., Spaapen R. M., Zha Y., et al. Up-regulation of PD-L1, IDO, and T(regs) in the melanoma tumor microenvironment is driven by CD8(+) T cells. Sci Transl Med. 2013; 5:200ra116. doi: 10.1126/scitranslmed.3006504.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Kinter A.L., Godbout E. J., McNally J.P., et al. The common gamma-chain cytokines IL-2, IL-7, IL-15, and IL-21 induce the expression of programmed death-1 and its ligands. J Immunol. 2008; 181:6738. doi: 10.4049/jimmunol.181.10.6738.</mixed-citation><mixed-citation xml:lang="en">Kinter A.L., Godbout E. J., McNally J.P., et al. The common gamma-chain cytokines IL-2, IL-7, IL-15, and IL-21 induce the expression of programmed death-1 and its ligands. J Immunol. 2008; 181:6738. doi: 10.4049/jimmunol.181.10.6738.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Yang J., Riella L. V., Chock S., et al. The novel costimulatory programmed death ligand 1/B7.1 pathway is functional in inhibiting alloimmune responses in vivo. J Immunol. 2011; 187:1113. doi: 10.4049/jimmunol.1100056.</mixed-citation><mixed-citation xml:lang="en">Yang J., Riella L. V., Chock S., et al. The novel costimulatory programmed death ligand 1/B7.1 pathway is functional in inhibiting alloimmune responses in vivo. J Immunol. 2011; 187:1113. doi: 10.4049/jimmunol.1100056.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Chambers C.A., Sullivan T. J., Allison J. P. Lymphoproliferation in CTLA-4-deficient mice is mediated by costimulation-dependent activation of CD4+ T cells. Immunity. 1997; 7:885. doi: 10.1016/s1074-7613(00)80406-9.</mixed-citation><mixed-citation xml:lang="en">Chambers C.A., Sullivan T. J., Allison J. P. Lymphoproliferation in CTLA-4-deficient mice is mediated by costimulation-dependent activation of CD4+ T cells. Immunity. 1997; 7:885. doi: 10.1016/s1074-7613(00)80406-9.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Tivol E.A., Borriello F., Schweitzer A. N., et al. Loss of CTLA-4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA-4. Immunity. 1995; 3:541. doi: 10.1016/1074-7613(95)90125-6.</mixed-citation><mixed-citation xml:lang="en">Tivol E.A., Borriello F., Schweitzer A. N., et al. Loss of CTLA-4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA-4. Immunity. 1995; 3:541. doi: 10.1016/1074-7613(95)90125-6.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Waterhouse P., Penninger J. M., Timms E., et al. Lymphoproliferative disorders with early lethality in mice deficient in Ctla-4. Science. 1995; 270:985. doi: 10.1126/science.270.5238.985.</mixed-citation><mixed-citation xml:lang="en">Waterhouse P., Penninger J. M., Timms E., et al. Lymphoproliferative disorders with early lethality in mice deficient in Ctla-4. Science. 1995; 270:985. doi: 10.1126/science.270.5238.985.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Walker L.S., Sansom D. M. The emerging role of CTLA4 as a cell-extrinsic regulator of T cell responses. Nat Rev Immunol. 2011; 11:852. doi: 10.1038/nri3108.</mixed-citation><mixed-citation xml:lang="en">Walker L.S., Sansom D. M. The emerging role of CTLA4 as a cell-extrinsic regulator of T cell responses. Nat Rev Immunol. 2011; 11:852. doi: 10.1038/nri3108.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Leach D.R., Krummel M. F., Allison J. P. Enhancement of antitumor immunity by CTLA-4 blockade. Science. 1996; 271:1734. doi: 10.1126/science.271.5256.1734.</mixed-citation><mixed-citation xml:lang="en">Leach D.R., Krummel M. F., Allison J. P. Enhancement of antitumor immunity by CTLA-4 blockade. Science. 1996; 271:1734. doi: 10.1126/science.271.5256.1734.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Schadendorf D., Hodi F. S., Robert C., et al. Pooled Analysis of Long-Term Survival Data From Phase II and Phase III Trials of Ipilimumab in Unresectable or Metastatic Melanoma. J Clin Oncol. 2015; 33:1889. doi: 10.1200/JCO.2014.56.2736.</mixed-citation><mixed-citation xml:lang="en">Schadendorf D., Hodi F. S., Robert C., et al. Pooled Analysis of Long-Term Survival Data From Phase II and Phase III Trials of Ipilimumab in Unresectable or Metastatic Melanoma. J Clin Oncol. 2015; 33:1889. doi: 10.1200/JCO.2014.56.2736.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Kisielow M., Kisielow J., Capoferri-Sollami G., Karjalainen K. Expression of lymphocyte activation gene 3 (LAG-3) on B cells is induced by T cells. Eur J Immunol. 2005; 35:2081. doi: 10.1002/eji.200526090.</mixed-citation><mixed-citation xml:lang="en">Kisielow M., Kisielow J., Capoferri-Sollami G., Karjalainen K. Expression of lymphocyte activation gene 3 (LAG-3) on B cells is induced by T cells. Eur J Immunol. 2005; 35:2081. doi: 10.1002/eji.200526090.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Grosso J.F., Goldberg M. V., Getnet D., et al. Functionally distinct LAG-3 and PD-1 subsets on activated and chronically stimulated CD8 T cells. J Immunol. 2009; 182:6659. doi: 10.4049/jimmunol.0804211.</mixed-citation><mixed-citation xml:lang="en">Grosso J.F., Goldberg M. V., Getnet D., et al. Functionally distinct LAG-3 and PD-1 subsets on activated and chronically stimulated CD8 T cells. J Immunol. 2009; 182:6659. doi: 10.4049/jimmunol.0804211.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Watanabe N., Gavrieli M., Sedy J. R., et al. BTLA is a lymphocyte inhibitory receptor with similarities to CTLA-4 and PD-1. Nat Immunol. 2003; 4:670. doi: 10.1038/ni944.</mixed-citation><mixed-citation xml:lang="en">Watanabe N., Gavrieli M., Sedy J. R., et al. BTLA is a lymphocyte inhibitory receptor with similarities to CTLA-4 and PD-1. Nat Immunol. 2003; 4:670. doi: 10.1038/ni944.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Murphy K.M., Nelson C. A., Sedý J. R. Balancing co-stimulation and inhibition with BTLA and HVEM. Nat Rev Immunol. 2006; 6:671. doi: 10.1038/nri1917.</mixed-citation><mixed-citation xml:lang="en">Murphy K.M., Nelson C. A., Sedý J. R. Balancing co-stimulation and inhibition with BTLA and HVEM. Nat Rev Immunol. 2006; 6:671. doi: 10.1038/nri1917.</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Fourcade J., Sun Z., Pagliano O., et al. CD8(+) T cells specific for tumor antigens can be rendered dysfunctional by the tumor microenvironment through upregulation of the inhibitory receptors BTLA and PD-1. Cancer Res. 2012; 72:887. doi: 10.1158/0008-5472.CAN-11-2637.</mixed-citation><mixed-citation xml:lang="en">Fourcade J., Sun Z., Pagliano O., et al. CD8(+) T cells specific for tumor antigens can be rendered dysfunctional by the tumor microenvironment through upregulation of the inhibitory receptors BTLA and PD-1. Cancer Res. 2012; 72:887. doi: 10.1158/0008-5472.CAN-11-2637.</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Lines J.L., Pantazi E., Mak J., et al. VISTA is an immune checkpoint molecule for human T cells. Cancer Res. 2014; 74:1924. doi: 10.1158/0008-5472.CAN-13-1504.</mixed-citation><mixed-citation xml:lang="en">Lines J.L., Pantazi E., Mak J., et al. VISTA is an immune checkpoint molecule for human T cells. Cancer Res. 2014; 74:1924. doi: 10.1158/0008-5472.CAN-13-1504.</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Wang L., Rubinstein R., Lines J. L., et al. VISTA, a novel mouse Ig superfamily ligand that negatively regulates T cell responses. J Exp Med. 2011; 208:577. doi: 10.1084/jem.20100619.</mixed-citation><mixed-citation xml:lang="en">Wang L., Rubinstein R., Lines J. L., et al. VISTA, a novel mouse Ig superfamily ligand that negatively regulates T cell responses. J Exp Med. 2011; 208:577. doi: 10.1084/jem.20100619.</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Le Mercier I., Chen W., Lines J. L., et al. VISTA Regulates the Development of Protective Antitumor Immunity. Cancer Res. 2014; 74:1933. doi: 10.1158/0008-5472.CAN-13-1506.</mixed-citation><mixed-citation xml:lang="en">Le Mercier I., Chen W., Lines J. L., et al. VISTA Regulates the Development of Protective Antitumor Immunity. Cancer Res. 2014; 74:1933. doi: 10.1158/0008-5472.CAN-13-1506.</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Monney L., Sabatos C. A., Gaglia J. L., et al. Th1-specific cell surface protein Tim-3 regulates macrophage activation and severity of an autoimmune disease. Nature. 2002; 415:536. doi: 10.1038/415536a.</mixed-citation><mixed-citation xml:lang="en">Monney L., Sabatos C. A., Gaglia J. L., et al. Th1-specific cell surface protein Tim-3 regulates macrophage activation and severity of an autoimmune disease. Nature. 2002; 415:536. doi: 10.1038/415536a.</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Anderson A.C., Anderson D. E., Bregoli L., et al. Promotion of tissue inflammation by the immune receptor Tim-3 expressed on innate immune cells. Science. 2007; 318:1141. doi: 10.1126/science.1148536.</mixed-citation><mixed-citation xml:lang="en">Anderson A.C., Anderson D. E., Bregoli L., et al. Promotion of tissue inflammation by the immune receptor Tim-3 expressed on innate immune cells. Science. 2007; 318:1141. doi: 10.1126/science.1148536.</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Zhu C., Anderson A. C., Schubart A., et al. The Tim-3 ligand galectin-9 negatively regulates T helper type 1 immunity. Nat Immunol. 2005; 6:1245. doi: 10.1038/ni1271.</mixed-citation><mixed-citation xml:lang="en">Zhu C., Anderson A. C., Schubart A., et al. The Tim-3 ligand galectin-9 negatively regulates T helper type 1 immunity. Nat Immunol. 2005; 6:1245. doi: 10.1038/ni1271.</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Sabatos C.A., Chakravarti S., Cha E., et al.Interaction of Tim-3 and Tim-3 ligand regulates T helper type 1 responses and induction of peripheral tolerance. Nat Immunol. 2003; 4:1102. doi: 10.1038/ni988.</mixed-citation><mixed-citation xml:lang="en">Sabatos C.A., Chakravarti S., Cha E., et al.Interaction of Tim-3 and Tim-3 ligand regulates T helper type 1 responses and induction of peripheral tolerance. Nat Immunol. 2003; 4:1102. doi: 10.1038/ni988.</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Ngiow S.F., von Scheidt B., Akiba H., et al. Anti-TIM3 antibody promotes T cell IFN-γ-mediated antitumor immunity and suppresses established tumors. Cancer Res. 2011; 71:3540. doi: 10.1158/0008-5472.CAN-11-0096.</mixed-citation><mixed-citation xml:lang="en">Ngiow S.F., von Scheidt B., Akiba H., et al. Anti-TIM3 antibody promotes T cell IFN-γ-mediated antitumor immunity and suppresses established tumors. Cancer Res. 2011; 71:3540. doi: 10.1158/0008-5472.CAN-11-0096.</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Advani R., Flinn I., Popplewell L., et al. CD47 Blockade by Hu5F9-G4 and Rituximab in Non-Hodgkin’s Lymphoma. N Engl J Med. 2018; 379:1711. doi: 10.1056/NEJMoa1807315.</mixed-citation><mixed-citation xml:lang="en">Advani R., Flinn I., Popplewell L., et al. CD47 Blockade by Hu5F9-G4 and Rituximab in Non-Hodgkin’s Lymphoma. N Engl J Med. 2018; 379:1711. doi: 10.1056/NEJMoa1807315.</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Wilcox R.A., Chapoval A. I., Gorski K. S., et al. Cutting edge: Expression of functional CD137 receptor by dendritic cells. J Immunol. 2002; 168:4262. doi: 10.4049/jimmunol.168.9.4262.</mixed-citation><mixed-citation xml:lang="en">Wilcox R.A., Chapoval A. I., Gorski K. S., et al. Cutting edge: Expression of functional CD137 receptor by dendritic cells. J Immunol. 2002; 168:4262. doi: 10.4049/jimmunol.168.9.4262.</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">McHugh R.S., Whitters M. J., Piccirillo C. A., et al. CD4(+)CD25(+) immunoregulatory T cells: gene expression analysis reveals a functional role for the glucocorticoid-induced TNF receptor. Immunity. 2002; 16:311. doi: 10.1016/s1074-7613(02)00280-7.</mixed-citation><mixed-citation xml:lang="en">McHugh R.S., Whitters M. J., Piccirillo C. A., et al. CD4(+)CD25(+) immunoregulatory T cells: gene expression analysis reveals a functional role for the glucocorticoid-induced TNF receptor. Immunity. 2002; 16:311. doi: 10.1016/s1074-7613(02)00280-7.</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Vinay D.S., Kwon B. S. 4-1BB signaling beyond T cells. Cell Mol Immunol. 2011; 8:281. doi: 10.1038/cmi.2010.82.</mixed-citation><mixed-citation xml:lang="en">Vinay D.S., Kwon B. S. 4-1BB signaling beyond T cells. Cell Mol Immunol. 2011; 8:281. doi: 10.1038/cmi.2010.82.</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Hernandez-Chacon J.A., Li Y., Wu R. C., et al. Costimulation through the CD137/4-1BB pathway protects human melanoma tumor-infiltrating lymphocytes from activation-induced cell death and enhances antitumor effector function. J Immunother. 2011; 34:236. doi: 10.1097/CJI.0b013e318209e7ec.</mixed-citation><mixed-citation xml:lang="en">Hernandez-Chacon J.A., Li Y., Wu R. C., et al. Costimulation through the CD137/4-1BB pathway protects human melanoma tumor-infiltrating lymphocytes from activation-induced cell death and enhances antitumor effector function. J Immunother. 2011; 34:236. doi: 10.1097/CJI.0b013e318209e7ec.</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Melero I., Shuford W. W., Newby S. A., et al. Monoclonal antibodies against the 4-1BB T-cell activation molecule eradicate established tumors. Nat Med. 1997; 3:682. doi: 10.1038/nm0697-682.</mixed-citation><mixed-citation xml:lang="en">Melero I., Shuford W. W., Newby S. A., et al. Monoclonal antibodies against the 4-1BB T-cell activation molecule eradicate established tumors. Nat Med. 1997; 3:682. doi: 10.1038/nm0697-682.</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">Uno T., Takeda K., Kojima Y., et al. Eradication of established tumors in mice by a combination antibody-based therapy. Nat Med. 2006; 12:693. doi: 10.1038/nm1405.</mixed-citation><mixed-citation xml:lang="en">Uno T., Takeda K., Kojima Y., et al. Eradication of established tumors in mice by a combination antibody-based therapy. Nat Med. 2006; 12:693. doi: 10.1038/nm1405.</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Takeda K., Kojima Y., Uno T., et al.Combination therapy of established tumors by antibodies targeting immune activating and suppressing molecules. J Immunol. 2010; 184:5493. doi: 10.1158/2326-6066.CIR-14-0007</mixed-citation><mixed-citation xml:lang="en">Takeda K., Kojima Y., Uno T., et al.Combination therapy of established tumors by antibodies targeting immune activating and suppressing molecules. J Immunol. 2010; 184:5493. doi: 10.1158/2326-6066.CIR-14-0007</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Youlin K., Jianwei Z., Xin G., et al. 4-1BB protects dendritic cells from prostate cancer-induced apoptosis. Pathol Oncol Res. 2013; 19:177. doi: 10.1007/s12253-012-9566-0.</mixed-citation><mixed-citation xml:lang="en">Youlin K., Jianwei Z., Xin G., et al. 4-1BB protects dendritic cells from prostate cancer-induced apoptosis. Pathol Oncol Res. 2013; 19:177. doi: 10.1007/s12253-012-9566-0.</mixed-citation></citation-alternatives></ref><ref id="cit74"><label>74</label><citation-alternatives><mixed-citation xml:lang="ru">Sznol M., Hodi F. S., Margolin K., et al. Phase I study of BMS-663513, a fully human anti-CD137 agonist monoclonal antibody in patients with advanced cancer (abstract 3007). American Society of Clinical Oncology meeting. 2008; 26:15_suppl, 3007-3007. doi: 10.1200/jco.2008.26.15_suppl.3007</mixed-citation><mixed-citation xml:lang="en">Sznol M., Hodi F. S., Margolin K., et al. Phase I study of BMS-663513, a fully human anti-CD137 agonist monoclonal antibody in patients with advanced cancer (abstract 3007). American Society of Clinical Oncology meeting. 2008; 26:15_suppl, 3007-3007. doi: 10.1200/jco.2008.26.15_suppl.3007</mixed-citation></citation-alternatives></ref><ref id="cit75"><label>75</label><citation-alternatives><mixed-citation xml:lang="ru">Segal N.H., He A. R., Doi T., et al. Phase I Study of Single-Agent Utomilumab (PF-05082566), a 4-1BB/CD137 Agonist, in Patients with Advanced Cancer. Clin Cancer Res 2018; 24:1816. doi: 10.1158/1078-0432.CCR-17-1922.</mixed-citation><mixed-citation xml:lang="en">Segal N.H., He A. R., Doi T., et al. Phase I Study of Single-Agent Utomilumab (PF-05082566), a 4-1BB/CD137 Agonist, in Patients with Advanced Cancer. Clin Cancer Res 2018; 24:1816. doi: 10.1158/1078-0432.CCR-17-1922.</mixed-citation></citation-alternatives></ref><ref id="cit76"><label>76</label><citation-alternatives><mixed-citation xml:lang="ru">Weinberg A.D., Morris N. P., Kovacsovics-Bankowski M., et al. Science gone translational: the OX40 agonist story. Immunol Rev 2011; 244:218. doi: 10.1111/j.1600-065X.2011.01069.x.</mixed-citation><mixed-citation xml:lang="en">Weinberg A.D., Morris N. P., Kovacsovics-Bankowski M., et al. Science gone translational: the OX40 agonist story. Immunol Rev 2011; 244:218. doi: 10.1111/j.1600-065X.2011.01069.x.</mixed-citation></citation-alternatives></ref><ref id="cit77"><label>77</label><citation-alternatives><mixed-citation xml:lang="ru">Takeda I., Ine S., Killeen N., et al. Distinct roles for the OX40-OX40 ligand interaction in regulatory and nonregulatory. T cells. J Immunol. 2004; 172:3580. doi: 10.4049/jimmunol.172.6.3580.</mixed-citation><mixed-citation xml:lang="en">Takeda I., Ine S., Killeen N., et al. Distinct roles for the OX40-OX40 ligand interaction in regulatory and nonregulatory. T cells. J Immunol. 2004; 172:3580. doi: 10.4049/jimmunol.172.6.3580.</mixed-citation></citation-alternatives></ref><ref id="cit78"><label>78</label><citation-alternatives><mixed-citation xml:lang="ru">Griseri T., Asquith M., Thompson C., Powrie F. OX40 is required for regulatory T cell-mediated control of colitis. J Exp Med. 2010; 207:699. doi: 10.1084/jem.20091618.</mixed-citation><mixed-citation xml:lang="en">Griseri T., Asquith M., Thompson C., Powrie F. OX40 is required for regulatory T cell-mediated control of colitis. J Exp Med. 2010; 207:699. doi: 10.1084/jem.20091618.</mixed-citation></citation-alternatives></ref><ref id="cit79"><label>79</label><citation-alternatives><mixed-citation xml:lang="ru">Valzasina B., Guiducci C., Dislich H., et al. Triggering of OX40 (CD134) on CD4(+)CD25+ T cells blocks their inhibitory activity: a novel regulatory role for OX40 and its comparison with GITR. Blood. 2005; 105:2845. doi: 10.1182/blood-2004-07-2959.</mixed-citation><mixed-citation xml:lang="en">Valzasina B., Guiducci C., Dislich H., et al. Triggering of OX40 (CD134) on CD4(+)CD25+ T cells blocks their inhibitory activity: a novel regulatory role for OX40 and its comparison with GITR. Blood. 2005; 105:2845. doi: 10.1182/blood-2004-07-2959.</mixed-citation></citation-alternatives></ref><ref id="cit80"><label>80</label><citation-alternatives><mixed-citation xml:lang="ru">Croft M. Control of immunity by the TNFR-related molecule OX40 (CD134). Annu Rev Immunol. 2010; 28:57. doi: 10.1146/annurev-immunol-030409-101243.</mixed-citation><mixed-citation xml:lang="en">Croft M. Control of immunity by the TNFR-related molecule OX40 (CD134). Annu Rev Immunol. 2010; 28:57. doi: 10.1146/annurev-immunol-030409-101243.</mixed-citation></citation-alternatives></ref><ref id="cit81"><label>81</label><citation-alternatives><mixed-citation xml:lang="ru">Weinberg A.D., Rivera M. M., Prell R., et al. Engagement of the OX-40 receptor in vivo enhances antitumor immunity. J Immunol. 2000; 164:2160. doi: 10.4049/jimmunol.164.4.2160.</mixed-citation><mixed-citation xml:lang="en">Weinberg A.D., Rivera M. M., Prell R., et al. Engagement of the OX-40 receptor in vivo enhances antitumor immunity. J Immunol. 2000; 164:2160. doi: 10.4049/jimmunol.164.4.2160.</mixed-citation></citation-alternatives></ref><ref id="cit82"><label>82</label><citation-alternatives><mixed-citation xml:lang="ru">Gough M.J., Crittenden M. R., Sarff M., et al. Adjuvant therapy with agonistic antibodies to CD134 (OX40) increases local control after surgical or radiation therapy of cancer in mice. J Immunother. 2010; 33:798. doi: 10.1097/CJI.0b013e3181ee7095.</mixed-citation><mixed-citation xml:lang="en">Gough M.J., Crittenden M. R., Sarff M., et al. Adjuvant therapy with agonistic antibodies to CD134 (OX40) increases local control after surgical or radiation therapy of cancer in mice. J Immunother. 2010; 33:798. doi: 10.1097/CJI.0b013e3181ee7095.</mixed-citation></citation-alternatives></ref><ref id="cit83"><label>83</label><citation-alternatives><mixed-citation xml:lang="ru">Pan P.Y., Zang Y., Weber K., et al. OX40 ligation enhances primary and memory cytotoxic T lymphocyte responses in an immunotherapy for hepatic colon metastases. Mol Ther. 2002; 6:528. doi: 10.1006/mthe.2002.0699.</mixed-citation><mixed-citation xml:lang="en">Pan P.Y., Zang Y., Weber K., et al. OX40 ligation enhances primary and memory cytotoxic T lymphocyte responses in an immunotherapy for hepatic colon metastases. Mol Ther. 2002; 6:528. doi: 10.1006/mthe.2002.0699.</mixed-citation></citation-alternatives></ref><ref id="cit84"><label>84</label><citation-alternatives><mixed-citation xml:lang="ru">Watanabe A., Hara M., Chosa E., et al.Combination of adoptive cell transfer and antibody injection can eradicate established tumors in mice - an in vivo study using anti-OX40mAb, anti-CD25mAb and anti-CTLA4mAb-. Immunopharmacol. Immunotoxicol. 2010; 32:238. doi: 10.3109/08923970903222355.</mixed-citation><mixed-citation xml:lang="en">Watanabe A., Hara M., Chosa E., et al.Combination of adoptive cell transfer and antibody injection can eradicate established tumors in mice - an in vivo study using anti-OX40mAb, anti-CD25mAb and anti-CTLA4mAb-. Immunopharmacol. Immunotoxicol. 2010; 32:238. doi: 10.3109/08923970903222355.</mixed-citation></citation-alternatives></ref><ref id="cit85"><label>85</label><citation-alternatives><mixed-citation xml:lang="ru">Hirschhorn-Cymerman D., Rizzuto G. A., Merghoub T., et al. OX40 engagement and chemotherapy combination provides potent antitumor immunity with concomitant regulatory T cell apoptosis. J Exp Med. 2009; 206:1103. doi: 10.1084/jem.20082205.</mixed-citation><mixed-citation xml:lang="en">Hirschhorn-Cymerman D., Rizzuto G. A., Merghoub T., et al. OX40 engagement and chemotherapy combination provides potent antitumor immunity with concomitant regulatory T cell apoptosis. J Exp Med. 2009; 206:1103. doi: 10.1084/jem.20082205.</mixed-citation></citation-alternatives></ref><ref id="cit86"><label>86</label><citation-alternatives><mixed-citation xml:lang="ru">Nocentini G., Ronchetti S., Petrillo M. G., Riccardi C. Pharmacological modulation of GITRL/GITR system: therapeutic perspectives. Br J Pharmacol. 2012; 165:2089. doi: 10.1111/j.1476-5381.2011.01753.x.</mixed-citation><mixed-citation xml:lang="en">Nocentini G., Ronchetti S., Petrillo M. G., Riccardi C. Pharmacological modulation of GITRL/GITR system: therapeutic perspectives. Br J Pharmacol. 2012; 165:2089. doi: 10.1111/j.1476-5381.2011.01753.x.</mixed-citation></citation-alternatives></ref><ref id="cit87"><label>87</label><citation-alternatives><mixed-citation xml:lang="ru">Schaer D.A., Murphy J. T., Wolchok J. D. Modulation of GITR for cancer immunotherapy. Curr Opin Immunol. 2012; 24:217. doi: 10.1016/j.coi.2011.12.011.</mixed-citation><mixed-citation xml:lang="en">Schaer D.A., Murphy J. T., Wolchok J. D. Modulation of GITR for cancer immunotherapy. Curr Opin Immunol. 2012; 24:217. doi: 10.1016/j.coi.2011.12.011.</mixed-citation></citation-alternatives></ref><ref id="cit88"><label>88</label><citation-alternatives><mixed-citation xml:lang="ru">Lacal P.M., Petrillo M. G., Ruffini F., et al. Glucocorticoid-induced tumor necrosis factor receptor family-related ligand triggering upregulates vascular cell adhesion molecule-1 and intercellular adhesion molecule-1 and promotes leukocyte adhesion. J Pharmacol Exp Ther. 2013; 347:164. doi: 10.1124/jpet.113.207605.</mixed-citation><mixed-citation xml:lang="en">Lacal P.M., Petrillo M. G., Ruffini F., et al. Glucocorticoid-induced tumor necrosis factor receptor family-related ligand triggering upregulates vascular cell adhesion molecule-1 and intercellular adhesion molecule-1 and promotes leukocyte adhesion. J Pharmacol Exp Ther. 2013; 347:164. doi: 10.1124/jpet.113.207605.</mixed-citation></citation-alternatives></ref><ref id="cit89"><label>89</label><citation-alternatives><mixed-citation xml:lang="ru">Shimizu J., Yamazaki S., Takahashi T., et al. Stimulation of CD25(+)CD4(+) regulatory T cells through GITR breaks immunological self-tolerance. Nat Immunol. 2002; 3:135. doi: 10.1038/ni759.</mixed-citation><mixed-citation xml:lang="en">Shimizu J., Yamazaki S., Takahashi T., et al. Stimulation of CD25(+)CD4(+) regulatory T cells through GITR breaks immunological self-tolerance. Nat Immunol. 2002; 3:135. doi: 10.1038/ni759.</mixed-citation></citation-alternatives></ref><ref id="cit90"><label>90</label><citation-alternatives><mixed-citation xml:lang="ru">Stephens G.L., McHugh R.S., Whitters M. J., et al. Engagement of glucocorticoid-induced TNFR family-related receptor on effector T cells by its ligand mediates resistance to suppression by CD4+CD25+ T cells. J Immunol. 2004; 173:5008. doi: 10.4049/jimmunol.173.8.5008.</mixed-citation><mixed-citation xml:lang="en">Stephens G.L., McHugh R.S., Whitters M. J., et al. Engagement of glucocorticoid-induced TNFR family-related receptor on effector T cells by its ligand mediates resistance to suppression by CD4+CD25+ T cells. J Immunol. 2004; 173:5008. doi: 10.4049/jimmunol.173.8.5008.</mixed-citation></citation-alternatives></ref><ref id="cit91"><label>91</label><citation-alternatives><mixed-citation xml:lang="ru">Ko K., Yamazaki S., Nakamura K., et al. Treatment of advanced tumors with agonistic anti-GITR mAb and its effects on tumor-infiltrating Foxp3+CD25+CD4+ regulatory T cells. J Exp Med. 2005; 202:885. doi: 10.1084/jem.20050940.</mixed-citation><mixed-citation xml:lang="en">Ko K., Yamazaki S., Nakamura K., et al. Treatment of advanced tumors with agonistic anti-GITR mAb and its effects on tumor-infiltrating Foxp3+CD25+CD4+ regulatory T cells. J Exp Med. 2005; 202:885. doi: 10.1084/jem.20050940.</mixed-citation></citation-alternatives></ref><ref id="cit92"><label>92</label><citation-alternatives><mixed-citation xml:lang="ru">Schaer D.A., Cohen A. D., Wolchok J. D. Anti-GITR antibodies - potential clinical applications for tumor immunotherapy. Curr Opin Investig Drugs. 2010; 11:1378. PMID: 21154120.</mixed-citation><mixed-citation xml:lang="en">Schaer D.A., Cohen A. D., Wolchok J. D. Anti-GITR antibodies - potential clinical applications for tumor immunotherapy. Curr Opin Investig Drugs. 2010; 11:1378. PMID: 21154120.</mixed-citation></citation-alternatives></ref><ref id="cit93"><label>93</label><citation-alternatives><mixed-citation xml:lang="ru">Cohen A.D., Schaer D. A., Liu C., et al. Agonist anti-GITR monoclonal antibody induces melanoma tumor immunity in mice by altering regulatory T cell stability and intra-tumor accumulation. PLoS One. 2010; 5: e10436. doi: 10.1371/journal.pone.0010436.</mixed-citation><mixed-citation xml:lang="en">Cohen A.D., Schaer D. A., Liu C., et al. Agonist anti-GITR monoclonal antibody induces melanoma tumor immunity in mice by altering regulatory T cell stability and intra-tumor accumulation. PLoS One. 2010; 5: e10436. doi: 10.1371/journal.pone.0010436.</mixed-citation></citation-alternatives></ref><ref id="cit94"><label>94</label><citation-alternatives><mixed-citation xml:lang="ru">Simpson T.R., Quezada S. A., Allison J. P. Regulation of CD4 T cell activation and effector function by inducible costimulator (ICOS). Curr Opin Immunol. 2010; 22:326. doi: 10.1016/j.coi.2010.01.001.</mixed-citation><mixed-citation xml:lang="en">Simpson T.R., Quezada S. A., Allison J. P. Regulation of CD4 T cell activation and effector function by inducible costimulator (ICOS). Curr Opin Immunol. 2010; 22:326. doi: 10.1016/j.coi.2010.01.001.</mixed-citation></citation-alternatives></ref><ref id="cit95"><label>95</label><citation-alternatives><mixed-citation xml:lang="ru">Fan X., Quezada S. A., Sepulveda M. A., et al. Engagement of the ICOS pathway markedly enhances efficacy of CTLA-4 blockade in cancer immunotherapy. J Exp Med. 2014; 211:715. doi: 10.1084/jem.20130590</mixed-citation><mixed-citation xml:lang="en">Fan X., Quezada S. A., Sepulveda M. A., et al. Engagement of the ICOS pathway markedly enhances efficacy of CTLA-4 blockade in cancer immunotherapy. J Exp Med. 2014; 211:715. doi: 10.1084/jem.20130590</mixed-citation></citation-alternatives></ref><ref id="cit96"><label>96</label><citation-alternatives><mixed-citation xml:lang="ru">Hassan S.B., Sørensen J. F., Olsen B. N., Pedersen A. E. Anti-CD40-mediated cancer immunotherapy: an update of recent and ongoing clinical trials. Immunopharmacol Immunotoxicol. 2014; 36:96. doi: 10.3109/08923973.2014.890626.</mixed-citation><mixed-citation xml:lang="en">Hassan S.B., Sørensen J. F., Olsen B. N., Pedersen A. E. Anti-CD40-mediated cancer immunotherapy: an update of recent and ongoing clinical trials. Immunopharmacol Immunotoxicol. 2014; 36:96. doi: 10.3109/08923973.2014.890626.</mixed-citation></citation-alternatives></ref><ref id="cit97"><label>97</label><citation-alternatives><mixed-citation xml:lang="ru">Suntharalingam G., Perry M. R., Ward S., et al. Cytokine storm in a phase 1 trial of the anti-CD28 monoclonal antibody TGN1412. N Engl J Med. 2006; 355:1018. doi: 10.1056/NEJMoa063842.</mixed-citation><mixed-citation xml:lang="en">Suntharalingam G., Perry M. R., Ward S., et al. Cytokine storm in a phase 1 trial of the anti-CD28 monoclonal antibody TGN1412. N Engl J Med. 2006; 355:1018. doi: 10.1056/NEJMoa063842.</mixed-citation></citation-alternatives></ref><ref id="cit98"><label>98</label><citation-alternatives><mixed-citation xml:lang="ru">Davila M.L., Brentjens R., Wang X., et al. How do CARs work?: Early insights from recent clinical studies targeting CD19. Oncoimmunology. 2012; 1:1577. doi: 10.4161/onci.22524.</mixed-citation><mixed-citation xml:lang="en">Davila M.L., Brentjens R., Wang X., et al. How do CARs work?: Early insights from recent clinical studies targeting CD19. Oncoimmunology. 2012; 1:1577. doi: 10.4161/onci.22524.</mixed-citation></citation-alternatives></ref><ref id="cit99"><label>99</label><citation-alternatives><mixed-citation xml:lang="ru">Sadelain M., Brentjens R., Rivière I. The basic principles of chimeric antigen receptor design. Cancer Discov. 2013; 3:388. doi: 10.1158/2159-8290.CD-12-0548.</mixed-citation><mixed-citation xml:lang="en">Sadelain M., Brentjens R., Rivière I. The basic principles of chimeric antigen receptor design. Cancer Discov. 2013; 3:388. doi: 10.1158/2159-8290.CD-12-0548.</mixed-citation></citation-alternatives></ref><ref id="cit100"><label>100</label><citation-alternatives><mixed-citation xml:lang="ru">Brentjens R.J., Davila M. L., Riviere I., et al. CD19-targeted T cells rapidly induce molecular remissions in adults with chemotherapy-refractory acute lymphoblastic leukemia. Sci Transl Med. 2013; 5:177ra38. doi: 10.1126/scitranslmed.3005930.</mixed-citation><mixed-citation xml:lang="en">Brentjens R.J., Davila M. L., Riviere I., et al. CD19-targeted T cells rapidly induce molecular remissions in adults with chemotherapy-refractory acute lymphoblastic leukemia. Sci Transl Med. 2013; 5:177ra38. doi: 10.1126/scitranslmed.3005930.</mixed-citation></citation-alternatives></ref><ref id="cit101"><label>101</label><citation-alternatives><mixed-citation xml:lang="ru">Grupp S.A., Kalos M., Barrett D., et al. Chimeric antigen receptor-modified T cells for acute lymphoid leukemia. N Engl J Med. 2013; 368:1509. doi: 10.1056/NEJMoa1215134.</mixed-citation><mixed-citation xml:lang="en">Grupp S.A., Kalos M., Barrett D., et al. Chimeric antigen receptor-modified T cells for acute lymphoid leukemia. N Engl J Med. 2013; 368:1509. doi: 10.1056/NEJMoa1215134.</mixed-citation></citation-alternatives></ref><ref id="cit102"><label>102</label><citation-alternatives><mixed-citation xml:lang="ru">Porter D.L., Hwang W. T., Frey N. V., et al. Chimeric antigen receptor T cells persist and induce sustained remissions in relapsed refractory chronic lymphocytic leukemia. Sci Transl Med. 2015; 7:303ra139. doi: 10.1126/scitranslmed.aac5415.</mixed-citation><mixed-citation xml:lang="en">Porter D.L., Hwang W. T., Frey N. V., et al. Chimeric antigen receptor T cells persist and induce sustained remissions in relapsed refractory chronic lymphocytic leukemia. Sci Transl Med. 2015; 7:303ra139. doi: 10.1126/scitranslmed.aac5415.</mixed-citation></citation-alternatives></ref><ref id="cit103"><label>103</label><citation-alternatives><mixed-citation xml:lang="ru">Geyer M.B., Rivière I., Sénéchal B., et al. Safety and tolerability of conditioning chemotherapy followed by CD19-targeted CAR T cells for relapsed/refractory CLL. JCI Insight. 2019; 5. doi: 10.1172/jci.insight.122627.</mixed-citation><mixed-citation xml:lang="en">Geyer M.B., Rivière I., Sénéchal B., et al. Safety and tolerability of conditioning chemotherapy followed by CD19-targeted CAR T cells for relapsed/refractory CLL. JCI Insight. 2019; 5. doi: 10.1172/jci.insight.122627.</mixed-citation></citation-alternatives></ref><ref id="cit104"><label>104</label><citation-alternatives><mixed-citation xml:lang="ru">Rosenberg S.A., Restifo N. P. Adoptive cell transfer as personalized immunotherapy for human cancer. Science. 2015; 348:62. doi: 10.1126/science.aaa4967.</mixed-citation><mixed-citation xml:lang="en">Rosenberg S.A., Restifo N. P. Adoptive cell transfer as personalized immunotherapy for human cancer. Science. 2015; 348:62. doi: 10.1126/science.aaa4967.</mixed-citation></citation-alternatives></ref><ref id="cit105"><label>105</label><citation-alternatives><mixed-citation xml:lang="ru">Lu Y.C., Yao X., Crystal J. S., et al. Efficient identification of mutated cancer antigens recognized by T cells associated with durable tumor regressions. Clin Cancer Res. 2014; 20:3401. doi: 10.1158/1078-0432.CCR-14-0433.</mixed-citation><mixed-citation xml:lang="en">Lu Y.C., Yao X., Crystal J. S., et al. Efficient identification of mutated cancer antigens recognized by T cells associated with durable tumor regressions. Clin Cancer Res. 2014; 20:3401. doi: 10.1158/1078-0432.CCR-14-0433.</mixed-citation></citation-alternatives></ref><ref id="cit106"><label>106</label><citation-alternatives><mixed-citation xml:lang="ru">Rosenberg S.A., Yang J. C., Sherry R. M., et al. Durable complete responses in heavily pretreated patients with metastatic melanoma using T-cell transfer immunotherapy. Clin Cancer Res. 2011; 17:4550. doi: 10.1158/1078-0432.CCR-11-0116.</mixed-citation><mixed-citation xml:lang="en">Rosenberg S.A., Yang J. C., Sherry R. M., et al. Durable complete responses in heavily pretreated patients with metastatic melanoma using T-cell transfer immunotherapy. Clin Cancer Res. 2011; 17:4550. doi: 10.1158/1078-0432.CCR-11-0116.</mixed-citation></citation-alternatives></ref><ref id="cit107"><label>107</label><citation-alternatives><mixed-citation xml:lang="ru">Liddy N., Bossi G., Adams K. J., et al. Monoclonal TCR-redirected tumor cell killing. Nat Med. 2012; 18:980. doi: 10.1038/nm.2764.</mixed-citation><mixed-citation xml:lang="en">Liddy N., Bossi G., Adams K. J., et al. Monoclonal TCR-redirected tumor cell killing. Nat Med. 2012; 18:980. doi: 10.1038/nm.2764.</mixed-citation></citation-alternatives></ref><ref id="cit108"><label>108</label><citation-alternatives><mixed-citation xml:lang="ru">Oates J., Hassan N. J., Jakobsen B. K. ImmTACs for targeted cancer therapy: Why, what, how, and which. Mol Immunol. 2015; 67:67. doi: 10.1016/j.molimm.2015.01.024.</mixed-citation><mixed-citation xml:lang="en">Oates J., Hassan N. J., Jakobsen B. K. ImmTACs for targeted cancer therapy: Why, what, how, and which. Mol Immunol. 2015; 67:67. doi: 10.1016/j.molimm.2015.01.024.</mixed-citation></citation-alternatives></ref><ref id="cit109"><label>109</label><citation-alternatives><mixed-citation xml:lang="ru">Cameron B.J., Gerry A. B., Dukes J., et al. Identification of a Titin-derived HLA-A1-presented peptide as a cross-reactive target for engineered MAGE A3-directed T cells. Sci Transl Med. 2013; 5:197ra103. doi: 10.1126/scitranslmed.3006034.</mixed-citation><mixed-citation xml:lang="en">Cameron B.J., Gerry A. B., Dukes J., et al. Identification of a Titin-derived HLA-A1-presented peptide as a cross-reactive target for engineered MAGE A3-directed T cells. Sci Transl Med. 2013; 5:197ra103. doi: 10.1126/scitranslmed.3006034.</mixed-citation></citation-alternatives></ref><ref id="cit110"><label>110</label><citation-alternatives><mixed-citation xml:lang="ru">de Gruijl T. D., Janssen A. B., van Beusechem V. W. Arming oncolytic viruses to leverage antitumor immunity. Expert Opin Biol Ther. 2015; 15:959. doi: 10.1517/14712598.2015.1044433.</mixed-citation><mixed-citation xml:lang="en">de Gruijl T. D., Janssen A. B., van Beusechem V. W. Arming oncolytic viruses to leverage antitumor immunity. Expert Opin Biol Ther. 2015; 15:959. doi: 10.1517/14712598.2015.1044433.</mixed-citation></citation-alternatives></ref><ref id="cit111"><label>111</label><citation-alternatives><mixed-citation xml:lang="ru">Ozao-Choy J., Lee D. J., Faries M. B. Melanoma vaccines: mixed past, promising future. Surg Clin North Am. 2014; 94:1017. doi: 10.1016/j.suc.2014.07.005</mixed-citation><mixed-citation xml:lang="en">Ozao-Choy J., Lee D. J., Faries M. B. Melanoma vaccines: mixed past, promising future. Surg Clin North Am. 2014; 94:1017. doi: 10.1016/j.suc.2014.07.005</mixed-citation></citation-alternatives></ref><ref id="cit112"><label>112</label><citation-alternatives><mixed-citation xml:lang="ru">UpToDate Principles of cancer immunotherapy</mixed-citation><mixed-citation xml:lang="en">UpToDate Principles of cancer immunotherapy</mixed-citation></citation-alternatives></ref><ref id="cit113"><label>113</label><citation-alternatives><mixed-citation xml:lang="ru">Yarilin A. A. Immunology. Moscow. GEOTAR-Media, 2010. 752 p. @@Иммунология / Ярилин А. А. - М.: ГЭОТАР-Медиа, 2010. - 752 с.</mixed-citation><mixed-citation xml:lang="en">Yarilin A. A. Immunology. Moscow. GEOTAR-Media, 2010. 752 p. @@Иммунология / Ярилин А. А. - М.: ГЭОТАР-Медиа, 2010. - 752 с.</mixed-citation></citation-alternatives></ref><ref id="cit114"><label>114</label><citation-alternatives><mixed-citation xml:lang="ru">Fundamentals of clinical immunology and allergology: textbook. ed. L. S. Namazova-Baranova, L. V. Gankovskaya, N. G. Astafieva. Moscow. Pediatr, 2016. 152 p. @@Основы клинической иммунологии и аллергологии: уч.пособие/ под ред. Л. С. Намазовой-Барановой, Л. В. Ганковской, Н.Г Астафьевой.-М.: ПедиатрЪ, 2016.-152 с.</mixed-citation><mixed-citation xml:lang="en">Fundamentals of clinical immunology and allergology: textbook. ed. L. S. Namazova-Baranova, L. V. Gankovskaya, N. G. Astafieva. Moscow. Pediatr, 2016. 152 p. @@Основы клинической иммунологии и аллергологии: уч.пособие/ под ред. Л. С. Намазовой-Барановой, Л. В. Ганковской, Н.Г Астафьевой.-М.: ПедиатрЪ, 2016.-152 с.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
